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ABSTRACT

The present invention concerns a cosmetic product for modifying the natural color of keratinous fibers, in particular human hair, comprising at least one packaging (VP) and a cosmetic composition (KM) contained in this packaging (VP). The packaging is made of a multi-layer film (F) comprising at least two polymer layers (P1) and (P2) and at least one barrier layer (BS). The cosmetic composition comprises at least one oxidizing agent, at least one C 8 -C 30  alcohol, at least one specific anionic surfactant, at least one non-ionic surfactant and at least one acrylic-based thickening agent. The use of the packaging (VP) in combination with the cosmetic composition (KM) does surprisingly not lead to an inflation of the packaging or an excessive water loss of the agent (KM) during storage.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a U.S. National-Stage entry under 35 U.S.C. § 371based on International Application No. PCT/EP2018/082264, filed Nov. 22,2018, which was published under PCT Article 21(2) and which claimspriority to German Application No. 10 2017 223 033.9, filed Dec. 18,2017, which are all hereby incorporated in their entirety by reference.

TECHNICAL FIELD

The present disclosure is in the field of cosmetics and concerns aproduct for oxidative color change of keratinous fibers, in particularhuman hair, which comprises an oxidant-containing composition packagedin a packaging. The oxidant-containing composition comprises at leastone C₈-C₃₀ alcohol, at least one specific anionic surfactant, at leastone non-ionic surfactant and at least one acrylic acid polymer asthickening agent. The packaging is made from a special multi-layer filmcomposite system, the wall of which comprises at least two polymericlayers and a barrier layer. The barrier layer has a penetration barriereffect for gases and water vapor. The barrier layer comprises a metal.

BACKGROUND

Changing the color of keratinous fibers, especially hair, is animportant area of modern cosmetics. The appearance of the hair may beadapted to current fashion trends as well as to the individual wishes ofeach person. The expert knows various methods for changing the color ofhair. The hair color may be changed temporarily by using direct dyes. Inthis process, already formed dyes diffuse from the dye into the hairfiber. Dyeing with direct dyes is associated with a low level of hairdamage, but a disadvantage is the low durability and the fastwashability of the colorations obtained with direct dyes.

If the consumer desires a long-lasting color result or a color shadethat is lighter than the original hair color, oxidative color modifiersare usually used. For permanent, intensive colorations withcorresponding fastness properties, so-called oxidative colorants areused. Such dyes usually contain oxidative colorant precursors, so-calleddeveloper components and coupler components, which form the actual dyesunder the influence of oxidants—usually hydrogen peroxides. Oxidativecolorants are exemplified by excellent, long-lasting dyeing results.

Oxidative color modifiers are usually marketed in the form oftwo-component agents, in which two different compositions are separatelypackaged in two separate packages and are not mixed together untilshortly before use. The first composition is a formulation—usuallyacidic for stability reasons—which contains, for example, hydrogenperoxide in concentrations of 1.5 to 12% by weight as an oxidizingagent. The oxidizing agent formulation is usually in the form of anemulsion or dispersion and is usually provided in a plastic bottle witha resealable outlet opening (developer bottle).

This oxidizing agent formulation is mixed with a second compositionbefore use. This second composition is an alkaline formulation which isoften in the form of a cream or a gel and which, if a color change isdesired at the same time as the brightening, also contains at least oneoxidative colorant precursor. This second composition may, for example,be provided in the form of a tube or in the form of a plastic or glasscontainer.

In the usual application form described above, the second composition,which contains the alkalizing agent and/or the oxidative colorantprecursors, is transferred from the tube or container into the developerbottle and then mixed by shaking with the hydrogen peroxide compositionalready in the developer bottle. In this way, the application mixture isprepared in the developer bottle. Application to the hair is thencarried out via a small spout or outlet opening at the top of thedeveloper bottle. The spout or outlet opening is opened after shakingand the application mixture may be removed by pressing the flexibledeveloper bottle.

The use of the developer bottle requires a certain routine from theuser, so that some users prefer to prepare the application mixture in amixing bowl and apply it with a brush.

When preparing the application mixture in a bowl, both components—thefirst composition containing the oxidizing agent and the secondcomposition containing an alkalizing agent and/or oxidative colorantprecursors—are completely transferred into a bowl or similar vessel andstirred there, for example with the aid of a brush. The applicationmixture is then removed from the mixing bowl using the brush. With thisform of application, the use of a voluminous and expensive developerbottle is not necessary, and the search continues for inexpensive andmaterial-saving packaging forms for the oxidizing agent composition.

In this context, packages in pocket or bag form, which are usually madeof plastic films or metal foils, are an inexpensive form of packagingwith low material consumption.

Such packaging may be produced, for example, by gluing or hot pressingtwo plastic foils lying one on top of the other, with the gluing takingplace on all edges of the foils. The interior of the packaging (i.e. theplastic bag) created by the bonding may then be filled with the desiredcosmetic composition. The packaging may be opened by tearing or cuttingopen the plastic bag.

However, filling oxidizing agent compositions into such packaging isassociated with problems caused by the reactivity of the oxidizingagent. Oxidizing agents are highly reactive substances which dependingon the storage conditions and the presence of decomposing impuritiesdecompose in small amounts and produce oxygen (i.e. gas).

The developer bottles known from the state of the art are usually onlyfilled with the oxidizing agent composition to a maximum of half,usually only to a third of their internal volume. As a rule, developerbottles are made of polyethylene. Since polyethylene is permeable toboth water vapor and other gases, there is no or only very slight excesspressure in the developer bottle. In addition, developer bottles areusually provided with strong, thick walls and a sturdy screw cap, sothat the diffusion of water vapor or gases through the thickness of thewalls is reduced and a slight increase in pressure within the bottle hasno negative effects.

In contrast, bag-shaped packages are usually completely filled with theliquid composition, and there is practically no excess air space in thefilled bag. In addition, such packages should be flexible, and whenopened (e.g. torn open or cut open) there should be no uncontrolledescape of the composition. For this reason, when packaging liquidcompositions, the creation of excess pressure in the package should beavoided if possible.

If an oxidizing agent composition is in such packaging, the gas (oxygen)produced during storage may cause the packaging to expand. Since theedges of the package are usually only glued together, in the worst case,strong inflation may lead to bursting of the packaging. For thesereasons, when storing oxidizing agent-containing compositions, thechoice of the film material of which the packaging is made is of greatimportance.

Packages made of pure plastic such as polyethylene or polypropylene arepermeable to both water vapor and gases. When storing a compositioncontaining oxidizing agents in a polyethylene or polypropylene package,the package does not expand. Due to the high permeability of thecomparatively thin film of the packaging to water vapor, however, thewater content of the composition is reduced. If the composition isstored in the packaging for several weeks or months, the water lossexceeds the maximum value permitted for adequate storage stability.

The production of suitable packaging for formulations containinghydrogen peroxide is a challenge. The above mentioned properties for thepermeability of oxygen and water vapor have to be adjusted in such a waythat a sufficient storage stability is given. The layer thickness of thefilm should be kept as low as possible for environmental reasons and topreserve resources. Furthermore, the layer thickness naturally also hasan influence on the manufacturing costs. Against this background, thinlayers are desired, but these do not always guarantee sufficientmechanical strength. If different materials are combined in amulti-layer film in order to satisfy a wide range of requirements, themanufactureability of the multi-layer film must also be guaranteed.Certain materials cannot be combined with each other because thecohesion between layers is not always sufficient or because theirprocessing temperatures may be so different that joint processing isdifficult.

Finally, the film materials are of great importance, especially whenstoring a multi-component system, as substances from the multi-componentsystem can diffuse into the films and promote the detachment of layersforming the film. The choice of components of a hydrogenperoxide-containing formulation therefore also has an impact on thechoice of packaging.

BRIEF SUMMARY

The objective of the present application was to package hydrogenperoxide-containing formulations in such a way that the mechanicalstrength of the packaging is sufficiently high to allow safe storage,but that easy access to the ingredients is guaranteed.

Surprisingly, it has now been found that oxidizing agent-containingcompositions may be packaged where the water vapor permeability is lowand inflation may be reduced by allowing the film to have a certainlevel of oxygen permeability. The films include a special film compositesystem and also have a barrier layer. By reducing the water vaporpermeability, but adjusting the oxygen permeability to a sufficientlyhigh level, the tendency to expand due to oxygen, which is formed fromthe hydrogen peroxide, is reduced and the mechanical strength isincreased over time.

In an exemplary embodiment, a cosmetic product for modifying the naturalcolor of keratinous fibers is provided. The cosmetic product includes atleast one packaging including at least one multi-layer film including atleast one first polymer layer, at least one second polymer layer and atleast one barrier layer. The cosmetic product further includes at leastone cosmetic composition packaged in the packaging. The at least onecosmetic composition includes at least one oxidizing compound, at leastone C8-C30 alcohol, at least one anionic surfactant selected fromcompounds of the formula R(OCH2CH2)n-OSO3-X+, wherein R representssaturated or unsaturated C8-C30 alkyl radicals, n represents integersfrom 10 to 50 and X+ represents a physiologically tolerable cation, atleast one non-ionic surfactant, and at least one thickening agentselected from the group of copolymers of (meth)acrylic acid and(meth)acrylic esters, copolymers of (meth)acrylates and(meth)acrylamides, copolymers of hydroxyethyl (meth)acrylates and(meth)acrylamides, copolymers of (meth)acrylates, (meth)acrylamides andethoxylated (meth)acrylic acid esters and mixtures thereof. The firstpolymer layer is formed of polyethylene terephthalate or polyethylenenaphthalate, the second polymer layer is formed of a polyolefin and thebarrier layer is formed of metalized, oriented polypropylene.

DETAILED DESCRIPTION

The following detailed description is merely exemplary in nature and isnot intended to limit the disclosure or the application and uses of thesubject matter as described herein. Furthermore, there is no intentionto be bound by any theory presented in the preceding background or thefollowing detailed description.

The subject-matter of the present disclosure is a cosmetic product forchanging the natural color of keratinous fibers, in particular humanhair, comprising

-   (i) at least one packaging (VP) comprising at least one multi-layer    film (F) comprising at least one first polymer layer (P1), at least    one second polymer layer (P2) and at least one barrier layer (BS),    and-   (ii) at least one cosmetic composition (KM) which is packaged in the    packaging (VP) and contains:    -   a) at least one oxidizing compound,    -   b) at least one C₈-C₃₀ alcohol,    -   c) at least one anionic surfactant selected from compounds of        the formula R(OCH₂CH₂)_(n)—OSO₃—X⁺, wherein R represents        saturated or unsaturated C₈-C₃₀ alkyl radicals, n represents        integers from 10 to 50 and X⁺ represents a physiologically        compatible cation,    -   d) at least one non-ionic surfactant; and    -   e) at least one thickening agent selected from the group of        copolymers of (meth)acrylic acid and (meth)acrylic esters,        copolymers of (meth)acrylates and (meth)acrylamides, copolymers        of hydroxyethyl (meth)acrylates and (meth)acrylamides,        Copolymers of (meth)acrylates, (meth)acrylamides and ethoxylated        (meth)acrylic acid esters and mixtures thereof, in particular        copolymers of (meth)acrylic acid and acrylic acid ethyl esters,        wherein the first polymer layer (P1) is formed of polyethylene        terephthalate or polyethylene naphthalate, in particular        polyethylene terephthalate; the second polymer layer (P2) is        formed of a polyolefin, in particular polyethylene; and the        barrier layer (BS) is formed of metalized, oriented        polypropylene.

Keratinous fibers, keratin-containing fibers or keratin fibers are furs,wool, feathers and in particular human hair. Although the products ascontemplated herein are primarily suitable for lightening and dyeingkeratinous fibers, there is nothing in principle to prevent their use inother areas.

The product as contemplated herein is a product for the oxidative colorchange of keratinous fibers, i.e. a product which is applied on thehuman head in order to achieve an oxidative coloring, a lightening, ableaching or a color nuance of the hair. In this context, color nuanceis understood to be a coloring in which the color result is lighter thanthe original hair color. That the product is to be used “to change thenatural color” means that the product either comprises only an oxidizingagent for bleaching, or that the product comprises an oxidizing agentused with a coupler that is not part of the present disclosure toachieve a color change, or that the product is used with a dye that isnot part of the present disclosure for further hair coloring.

Furthermore, the term “packaging” is understood to mean, as contemplatedherein, a packaging which is preferably in the form of a sachet. Asachet is a small package in the form of a bag or pouch, which is oftenused in the packaging of cosmetics. The capacity of the packaging, inparticular of the sachet, may, for example, be from about 5 to about1000 ml, preferably from about 10 to about 200 ml and particularlypreferably from about 20 to about 50 ml.

In addition, a multi-layer film (F) in the context of the presentdisclosure is understood to be a thin, flat and windable strip includingthe at least one polymer layer (P1) and the at least one polymer layer(P2). This multi-layer film (F) forms the wall of the packaging (VP).The packaging also comprises a barrier layer (BS), which selectivelypermits or reduces the passage of water vapor and other gases such asoxygen.

As contemplated herein, the permeability values of the film (F) are setto be advantageous. The film (F) thus provides the packaging withadvantageous barrier properties, in particular with respect to the WaterVapor Transmission Rate (WVTR, measured in g/(m²d) or g/(m²24 h))measured according to the ASTM F 1249 method at 38° C. ambienttemperature and 100% relative humidity, and for oxygen (OTR, oxygentransmission rate; measured in cm³/(m²d bar) or cm³/(m² 24 h), where cm³is equal to cc, at an atmospheric pressure of 1 bar) measured accordingto the ASTM D 3985 method at 23° C. ambient temperature and 50% relativehumidity.

Furthermore, as contemplated herein, the term “non-ionic surfactant” isunderstood to mean amphiphilic (bifunctional) compounds which have atleast one hydrophobic and at least one hydrophilic part of the molecule.The hydrophobic radical is preferably a hydrocarbon chain with 8 to 28carbon atoms, which may be saturated or unsaturated, linear or branched.This C₈-C₂₈ alkyl chain is particularly preferred linear. In contrast toanionic, cationic, zwitterionic and amphiphilic surfactants, however,non-ionic surfactants contain neither cationic nor anionic groups.Furthermore, these surfactants do not have any cationizable andanionizable groups which may form cationic or anionic groups dependingon the pH value.

Finally, in the context of the present disclosure, the term “thickeningagent” means compounds capable of binding liquids, in particular water,and increasing the viscosity of those liquids. In the context of thepresent disclosure, this also includes gel formers which are capable ofthickening liquids into compositions with a gel-like consistency or intogels. As contemplated herein, gel-like cosmetic products or gels aredimensionally stable, easily deformable disperse systems including atleast two components, the gel former (usually a solid, colloid-dividedsubstance with long or highly branched compounds) and a liquid (usuallywater) as dispersion agent. The gel former forms a spatial network inthe liquid, whereby the individual gel-forming compounds adhere to oneanother at different spatial points by major and/or minor valences. Inthis context, the term (meth)acrylate refers to both methacrylates andacrylates. Suitable thickening agents are, for example, the thickeningagents available under the following INCI designations: AcrylatesCopolymer, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer,Hydroxyethyl Acrylate Sodium Acryloyldimethyl Taurate Copolymer,Polyacrylate Crosspolymer 6, Ammonium Acryloyl Dimethyl Taurate(NH₄AMPS), Dimethyl Acrylamide, Lauryl Methacrylate and Laureth-4Methacrylate.

The cosmetic product as contemplated herein comprises as first componenta packaging (VP) comprising at least one multi-layer film (F). This filmcomprises at least one first polymer layer (P1), at least one secondpolymer layer (P2) and at least one barrier layer (BS). This multi-layerfilm forms the wall or outer shell of the packaging. As described above,such packaging is usually made by gluing, pressing or welding two piecesof film on top of each other (the packaging (VP) is filled with thecosmetic composition (KM) at the same time). i.e. such packaging isclosed at all edges. This packaging may be opened, for example, bytearing or cutting it open.

The thickness of the multi-layer film (F) determines the mechanicalproperties and the strength of the films. It should be designed in sucha way that there is sufficient mechanical stability, but at the sametime the film (F)—and thus the packaging (VP) produced from the filmshould be flexible enough to allow complete removal of the cosmeticcomposition (KM) from the opened packaging (VP) by pressing orsqueezing. A film meets these requirements if the film (F) has a certaintotal thickness. Preferred embodiments of the present disclosure atleast one multi-layer film has a total thickness of from about 28 μm toabout 220 μm, preferably of from about 52 μm to about 180 μm, morepreferably of from about 80 μm to about 140 μm. For the purposes of thepresent disclosure, the total thickness of the film (F) is understood tobe the sum of the thicknesses of all individual layers of which the film(F) consists.

The configuration of layers (P1), (P2) and (BS) within the multi-layerfilm (F) may be different. Furthermore, it is also possible that thefilm (F) includes further layers in addition to the layers mentionedabove. In addition, as contemplated herein, it is advantageous if allthe previously mentioned layers are oriented parallel to the surfaces ofthe film (F), i.e. all layers have the same orientation. If themulti-layer film (F) contains the three layers (P1), (P2) and (BS)described above, the following layouts of the layers would be possible(viewed from the interior (in contact with the cosmetic composition(KM)) to the exterior):

-   a) *Interior*-Layer (P1)-Layer (P2)-Barrier layer (BS)-*Exterior*,-   b) *Interior*-Layer (P1)-Barrier layer (BS)-Layer (P2)-*Exterior*,-   c) *Interior*-Layer (P2)-Layer (P1)-Barrier layer (BS)-*Exterior*,-   d) *Interior*-Layer (P2)-Barrier layer (BS)-Layer (P1)-*Exterior*,-   e) *Interior*-Barrier layer (BS)-Layer (P1)-Layer (P2)-*Exterior*,-   f) *Interior*-Barrier layer (BS)-Layer (P2)-Layer (P1)-*Exterior*.

However, as contemplated herein, it is preferred when the barrier layer(BS) is located between the first polymer layer (P1) and the secondpolymer layer (P2), the second polymer layer (P2) being located on theexterior of the package. In this case, the multi-layer film (F) iscomposed of three layers, layer (P1) being at the innermost and incontact with the cosmetic composition (KM). Layer (P1) is in contactwith the barrier layer (BS), and the barrier layer (BS) is in contactwith layer (P2). In this layer, the layers (P1) and (P2) are notadjacent to each other but are separated by the barrier layer (BS). Theparticular advantage of this configuration is that the—often verythin—barrier layer (BS) is not located on either the inner or outersurface of the multi-layer film (F), but is protected by the polymericlayer (P1) towards the inside and by the polymeric layer (P2) towardsthe outside. In this way, mechanical abrasion or destruction of thebarrier layer (BS) may be avoided as far as possible. It is thereforeadvantageous in the context of the present disclosure if the at leastone multi-layer film (F) contains the at least one barrier layer (BS)between the at least one first polymer layer (P1) and the at least onesecond polymer layer (P2). The use of such packaging has been shown tobe particularly advantageous in terms of increased storage stability, asthis layout shows neither swelling nor delamination during prolongedcontact with an an oxidizing agent-containing composition. In a furtherpreferred embodiment, the barrier layer (BS) is also located between thetwo polymer layers P1 and P2, but the first polymer layer (P1) islocated on the exterior of the package.

As contemplated herein, the exterior of the packaging (VP) is understoodto be that side of the packaging which does not come into contact withthe cosmetic composition (KM) but with the environment. The use of suchpackaging has proven to be particularly advantageous in terms ofincreased storage stability, as this layout shows neither swelling nordelamination during prolonged contact with an oxidizing agent-containingcomposition.

The first polymeric material of the first layer (P1) is, as contemplatedherein, a polyester. This material may be a layer of one polymer type ora layer of a polymer blend. According to the present disclosure, the atleast one first polymer layer (P1) is formed from polyethyleneterephthalate or polyethylene naphthalate, in particular frompolyethylene terephthalate. As contemplated herein, the term “formed” isunderstood to mean that the polymer layer contains at least about 70% byweight, preferably at least about 80% by weight, more preferably atleast about 90% by weight, most preferably at least about 99% by weight,in each case based on the total weight of the polymer layer (P1), of theabove-mentioned compounds.

Polyethylene terephthalate (PET) is a polymer from the polyester group.Polyethylene terephthalate may be produced, for example, bytransesterification of dimethyl terephthalate with ethylene glycol athigher temperatures. In this transesterification reaction, methanol issplit off, which is removed by distillation. The resultingbis(2-hydroxyethyl)-terephthalate is converted to PET bypolycondensation, again producing ethylene glycol. Another method ofproducing polyethylene terephthalate is the direct polycondensation ofethylene glycol and terephthalic acid at high temperatures withdistillation of the resulting water. Polyethylene terephthalate isexemplified by a particularly high mechanical strength. If the PET layerforms the outer layer, this also offers the advantage that the layersunderneath may be printed without the print being rubbed off. The PETlayer is transparent and provides a mechanical protective layer for theprinted layer.

According to a preferred embodiment of the present disclosure, the layerthickness of the first polymer layer (P1) is from about 4 μm to about 50μm, preferably from about 5 μm to about 35 μm, more preferably fromabout 6 μm to about 20 μm. The layer thickness of the PET layer usedaccording to the preferred embodiment of the present disclosure isassociated with special advantages, which are related to generalproperties of PET. PET is exemplified by high dimensionalstability/stiffness. If PET with these layer thicknesses is chosen asthe first polymer layer (P1), this offers an advantageous mechanicaldimensional stability for the film. At the same time, the overallthickness of the film may be kept low, so that a material andresource-saving film may be provided.

Furthermore, the multi-layer film (F) from which the package is madecomprises a second polymer layer (P2) of a second polymeric material.The second polymeric material may be a layer of one type of polymer or alayer of a polymer mixture. It is provided in the context of the presentdisclosure that the at least one second polymer layer (P2) is formed ofa polyolefin, in particular of polyethylene. As contemplated herein, theterm “formed” is understood to mean that the polymer layer comprises atleast about 70% by weight, preferably at least about 80% by weight, morepreferably at least about 90% by weight, in particular at least about99% by weight, each relative to the total weight of the polymer layer(P2) of the aforementioned compounds.

The second polymeric material of the second layer (P2) of themulti-layer film (F) is a polyolefin, in particular polyethylene.Polyolefins are polymers which are produced from alkenes such asethylene, propylene, 1-butene or isobutene by chain polymerization.Polyolefins are saturated hydrocarbons. They are semi-crystallinethermoplastics which are easy to process. They are exemplified by goodchemical resistance. Polyethylene and polypropylene are widely used infilm applications. As contemplated herein, polypropylene is thereforeused for the second layer (P2), but polyethylene is preferred.Polyethylene is produced by polymerization of ethylene using variouscatalysts. For example, polyethylene may be produced by polymerizingethylene in the gas phase or in suspension. The average relative molarmass may be controlled, for example, by adjusting a certain hydrogenpartial pressure during the polymerization of ethylene. Polyethylene maybe processed by extrusion and stretch blow molding, or by pressing,calendering, thermoforming and cold forming.

The second polymer layer (P2) serves as a supporting layer. Althoughpolyethylene has the disadvantage of being permeable to oxygen and watervapor, it has the advantage of being inexpensive and, due to its lowmelting point—lower than that of polypropylene—it is easy andenergy-saving to process.

According to a preferred embodiment of the present disclosure, thesecond polymer layer (P2) has a certain layer thickness. According tothe preferred embodiment of the present disclosure, the second polymerlayer (P2) has a layer thickness of from about 20 μm to about 150 μm,preferably of from about 30 μm to about 110 μm, more preferably of fromabout 40 μm to about 90 μm. In particular, the second polymer layer (P2)has a higher layer thickness than the first polymer layer (P1).

The polymer layers (P1) and (P2) of the multi-layer film (F) compriseorganic polymeric materials, which generally have only an insufficientbarrier effect against gases and water vapor. If the oxidizingagent-containing composition (KM) is packaged in a packaging (VP) madeof a multi-layer film (F), which only comprises the two organic polymerlayers (P1) and (P2), water vapor may escape unhindered, so that thewater content in the composition (KM) changes in an unacceptable wayduring longer storage. To minimize the uncontrolled escape of watervapor from the packaging (VP), the organic polymer layers (P1) and (P2)are therefore used in combination with a barrier layer (BS).

The barrier layer (BS) has a passage barrier effect for gases and watervapor. As contemplated herein, this means that the barrier layer (BS)reduces and controls the permeation rate of water vapor and gasesthrough the film. A film (F) as contemplated herein, which has a barrierlayer (BS) in addition to the layers (P1) and (P2), thus has a reducedwater vapor permeability and a reduced gas permeability compared to acomparable film (with the same overall thickness), which only has thetwo layers (P1) and (P2) but no barrier layer (BS).

For example, the barrier layer (BS) is a thin layer comprising aninorganic material, which may be applied to organic polymer layers usingvapor deposition techniques (e.g. PVD “physical vapor deposition” or CVD“chemical vapor deposition”).

If the barrier layer (BS) is a layer comprising at least one inorganicmaterial, then the films may be made of metals, semi-metals or metal orsemi-metal oxides, for example aluminum, aluminum oxides, magnesium,magnesium oxides, silicon, silicon oxides, titanium, titanium oxides,tin, tin oxides, zirconium, zirconium oxide and/or carbon.

As contemplated herein, the barrier layer (BS) is made of metallized,oriented polypropylene. Polypropylene is alternatively also known aspoly(1-methylethylene), and is a thermoplastic polymer belonging to thegroup of polyolefins. Polypropylene is produced by polymerization ofpropylene (propene) using various catalysts. For example, polypropylenecan be produced by stereospecific polymerization of propylene in the gasphase or in suspension according to Giulio Natta. Polypropylene ascontemplated herein may be isotactic and thus highly crystalline, butalso syndiotactic or amporphous. The average relative molar mass may becontrolled, for example, by adjusting a certain hydrogen partialpressure during the polymerization of the propene. For example,polypropylene may have average relative molar masses of approx. 150,000to 1,500,000 g/mol. Polypropylene may be processed by extrusion andstretch blow molding, or by pressing, calendering, thermoforming andcold forming.

An oriented polypropylene is defined by the expert as a polypropylenefilm which is stretched during production after an extrusion orcalendering step, namely stretched in the direction of extrusion and/orstretched at about 900 to the direction of extrusion. The film ispreferably stretched in both directions, i.e. films in which the barrierlayer—or the entire film—is biaxially stretched, particularly preferablysimultaneously biaxially. During the stretching step the polymericmaterial is oriented. This is of great importance for the properties ofthe film layer, especially in the case of polypropylenes, since theorientation step determines the shape of the crystalline domains of thepolymeric material and thus the physical properties of the film.

The polypropylene film is metallized. Possible metals are the abovementioned metals aluminum, magnesium, silicon, titanium, tin, andzirconium, especially aluminum. The metals are evaporated onto thecarrier film. According to a preferred embodiment of the presentdisclosure, the ratio of the layer thickness of metal to orientedpolypropylene is from about 1:1000 to about 1:10, preferably from about1:500 to about 1:50, more preferably from about 1:200 to about 1:100.

The production of films with barrier layers comprising inorganicmaterial is known. Also the multi-layer film (F) used as contemplatedherein may be manufactured by a process which is used for themanufacture of known films with barrier layers in the state of the art,as described for example in the documents EP 1036813 A1, EP 2371539 A1and EP 1541340 A1.

The barrier layer (BS) may additionally include a thin layer ofinorganic-organic hybrid polymers. These polymers are known in theliterature under the technical term ORMOCER polymers. A typical ORMOCERpolymer may be produced, for example, by hydrolytic polycondensation ofan organo-functional silane with an aluminum compound and possibly withan inorganic oxide component. Corresponding syntheses are disclosed inEP 0792846 B1, which is referred to in full here. Inorganic-organichybrid polymers (ORMOCER polymers) have both inorganic and organicnetwork structures. The inorganic silicate network structure may beformed in the sol-gel process by controlled hydrolysis and condensationof alkoxysilanes. The silicate network may be specifically modified byincluding metal alkoxides in the sol-gel process. By polymerization oforgano-functional groups, which are introduced into the material by theorganoalkoxylanes, an additional organic network is built up. TheORMOCER polymers produced in this way may be applied to layers (P1)and/or (P2) using conventional application techniques (spraying,brushing, etc.).

The thicker the barrier layer (BS), the greater or stronger the barriereffect against the passage of gases and water vapor. The thickness ofthe barrier layer (BS) may therefore be selected depending on thedesired barrier effect. According to a preferred embodiment of thepresent disclosure, the at least one barrier layer (BS) has a layerthickness of from about 4 μm to about 25 μm, preferably of from about 5μm to about 20 μm, more preferably of from about 6 μm to about 18 μm.

The material, structure and layer thicknesses determine the permeabilityvalues of the film. The multi-layer film (F) of the packaging of thecosmetic product as contemplated herein is exemplified by advantageousproperties with regard to oxygen permeability and water vaporpermeability. The multi-layer film exhibits an oxygen transmission rate(OTR) at about 23° C. and about 50% relative humidity of from about 0.1to about 5 cc/m²/d/bar, preferably from about 0.2 to about 3.5cc/m²/d/bar, more preferably from about 0.5 to about 2.5 cc/m²/d/bar,and a water vapor transmission rate at about 38° C. and about 100%relative humidity of from about 0.1 to about 5 g/m²d, preferably fromabout 0.2 to about 3.5 g/m²d, more preferably from about 0.5 to about2.5 g/m²d.

As contemplated herein, the permeability values of the film (F) areadvantageously adjusted. The film (F) thus imparts advantageous barrierproperties to the package, especially with regard to the permeabilityfor water vapor: Water Vapor Transmission Rate (WVTR) measured in theunit g/(m²d) or g/(m²24 h) measured according to the ASTM F 1249 methodat 38° C. ambient temperature and 100% relative humidity, and foroxygen: Oxygen Transmission Rate (OTR) measured in cm³/(m²d bar) orcm³/(m²24 h), where cm³ is equal to cc, at an atmospheric pressure of 1bar measured according to ASTM D 3985 at 23° C. ambient temperature and50% relative humidity.

In addition to the layers (P1), (P2) and (BS) described so far, themulti-layer film (F) may additionally comprise one or more furtherlayers. These additional layers may, for example, be intermediate layersand/or adhesive layers. It is therefore preferred as contemplated hereinif the at least one multi-layer film (F) additionally contains at leastone further layer selected from the group of intermediate layers (SZ),adhesive layers (SK) and mixtures thereof.

For example, the films (F) may have further intermediate layers (SZ) toincrease the mechanical stability. Intermediate layers may also preventor minimize the permeation of polymers or remaining monomers from apolymer layer into the cosmetic composition (KM).

To increase bond strength, the films may also comprise one or moreadhesive layers (SK) to reduce or prevent delamination (i.e. peeling orformation of an air space) between two layers.

A particularly preferred product as contemplated herein multi-layer film(F) comprises, in addition to the first polymer layer (P1), the secondpolymer layer (P2) and the barrier layer (BS), one or more furtherlayers selected from intermediate layers (SZ) and/or adhesive layers(SK).

If the multi-layer film (F) contains other layers in addition to thelayers (P1), (P2) and (BS), the following layouts of the layers arepossible (from interior (in contact with the cosmetic composition (KM))to exterior):

-   a) *Interior*-Layer (P1)-First adhesive layer (SK1)-Layer    (P2)-Second adhesive layer (SK2)-Barrier layer (BS)-*Exterior*,-   b) *Interior*-Layer (P1)-Adhesive layer (SK1)-Layer (P2)-Barrier    layer (BS)-*Exterior*,-   c) *Interior*-Layer (P1)-Layer (P2)-Second adhesive layer    (SK2)-Barrier layer (BS)-*Exterior*,-   d) *Interior*-Barrier layer (BS)-First adhesive layer (SK1)-Layer    (P1)-Second adhesive layer (SK2)-Layer (P2)-*Exterior*,-   e) *Interior*-Barrier layer (BS)-Adhesive layer (SK)-Layer    (P1)-Layer (P2)-*Exterior*,-   f) *Interior*-Barrier layer (BS)-Layer (S1)-Adhesive layer    (SK)-Layer (P2)-*Exterior*,-   g) *Interior*-Layer (P1)-First adhesive layer (SK1)-Barrier layer    (BS)-Second adhesive layer (SK2)-Layer (P2)-*Exterior*,-   h) *Interior*-Layer (P1)-Adhesive layer (SK)-Barrier layer    (BS)-Layer (P2)-*Exterior*,-   i) *Interior*-Layer (P1)-Barriere Layer (BS)-Adhesive layer    (SK)-Layer (P2)-*Exterior*

In any case, the film should be designed so that there is sufficientadhesion between the films. According to a preferred embodiment of thepresent disclosure, the bond strength of the film is from about 0.1 toabout 10 N/15 mm, preferably from about 1 to about 8 N/15 mm, morepreferably from about 1.5 to about 5 N/15 mm. This is measured by theASTM F-904 method. The bond strength is a physical measure of theadhesive force between the layers. It is related to the two layers of afilm with the lowest bond strength between two layers of the same film.The adhesive strengths set as contemplated herein result in a favorablemechanical stability over the storage time of the packaged cosmeticproduct.

Also, the strength between two bonded (sealed or sealed-off) filmsshould be sufficient. According to a preferred embodiment of the presentdisclosure, the seal strength of the packaging (VP) is from about 10 toabout 40 N/15 mm, preferably from about 15 to about 35 N/15 mm, morepreferably from about 20 to about 30 N/15 mm, under the conditions of150° C., 2.54 cm (1″) and 4 kg/cm2. The seal strength is measuredaccording to ASTM F-88 under the above conditions. The challenge withpackaging is always to ensure the mechanical durability of the packagingwhile at the same time making the contents easily accessible to theuser. Adjusting the seal strength to these values enables both of theseobjectives to be achieved.

The term sealed seam refers to a seam by which the package is closed.Usually, two films are placed on top of each other for closing thepackage and are pressed together by a force perpendicular to the filmsurface. By heating the films in the area that is being compressed,parts of the compressed areas may fuse together, so that the films arewelded together. There may also be an adhesive between the compressedfilms that strengthens the seam.

The product as contemplated herein comprises as a second component acosmetic composition (KM) which is packaged in the packaging (VP) whichcontains at least one oxidizing agent, at least one C₈-C₃₀ alcohol, atleast one specific anionic surfactant, at least one non-ionic surfactantand at least one acrylic acid polymer as thickening agent.

The intended use of the product as contemplated herein is oxidativecolor change. For this purpose—as already described above—a cosmeticcomposition (KM) containing an oxidizing agent is usually mixed with asecond composition (B) which is prepared separately from (KM). In thisway, the ready-to-use oxidative color changing agent is produced.Depending on whether the oxidative color change is intended to achieve ableaching, brightening or coloring effect, the composition (B) maycontain different ingredients. If pure lightening or bleaching is to beachieved, composition (B) contains at least one alkalizing agent. Ifoxidative coloration is desired, the composition (B) often contains theoxidative colorant precursors in addition to the alkalizing agent. Inorder to ensure that the compositions (KM) and (B) may be mixedsufficiently quickly, both the composition (KM) and the composition (B)are usually free-flowing, aqueous or water-containing compositions.

As contemplated herein, the composition (KM) is an aqueous composition.The water content of the composition (KM) may, for example, be fromabout 60 to about 97% by weight, preferably from about 75 to about 93%by weight, more preferably from about 78 to about 91% by weight, inparticular from about 80 to about 88.0% by weight, based on the totalweight of the composition (KM). All weight data in % by weight refer tothe total weight of water contained in the composition (KM), which isset in relation to the total weight of the composition (KM).

The cosmetic composition (KM) contains as first essential ingredient a)at least one oxidizing agent. Preference is given to certain oxidizingagents. It is therefore advantageous in the context of the presentdisclosure if the cosmetic composition (KM) contains at least oneoxidizing compound selected from the group of persulfates, chlorites,hydrogen peroxides and attachment products of hydrogen peroxides tourea, melamine and sodium borate, in particular hydrogen peroxides. Ascontemplated herein, the use of hydrogen peroxide has proven to beparticularly advantageous.

The concentration of the oxidizing agent in the composition (KM) isdetermined on the one hand by the legal requirements and on the otherhand by the desired effect; preferably from about 0.5 to about 20.0% byweight solutions in water are used. Therefore, it is found to bepreferred if the cosmetic composition (KM) contains at least oneoxidizing compound, in particular hydrogen peroxide, in a total amountof from about 0.5 to about 20% by weight, preferably from about 1.0 toabout 18% by weight, more preferably from about 1.2 to about 16.0% byweight, in particular from about 1.5 to about 15.0% by weight, based onthe total weight of the cosmetic composition (KM). The higher thecontent of oxidizing agent, in particular hydrogen peroxide, in thecomposition (KM), the greater is the amount of gas produced in the caseof a proportional decomposition of the oxidizing agent. Compositionscontaining a higher concentration of oxidizing agent are therefore muchmore difficult to package in packaging (VP) than compositions containinga lower concentration of oxidizing agent. The amount of hydrogenperoxide refers to about 100% hydrogen peroxide.

In the course of the work leading to this present disclosure, it wasfound that the product as contemplated herein is particularly suitablefor the packaging and stable storage of higher concentrated hydrogenperoxide compositions (KM). Thus, packaging (VP) as contemplated herein,which contained compositions (KM) with from about 9 to about 12% byweight of hydrogen peroxide, showed no changes in volume (i.e. noswelling) and no unplanned openings (i.e. the packages did not burstopen) even after storage at elevated temperature for several weeks.

The cosmetic composition (KM) contains as second essential ingredient b)at least one C₈-C₃₀ alcohol. In this context, mixtures of linear C₁₄-C₁₈alcohols have proved particularly effective. Such mixtures, incombination with the further features c) to e) of the composition (KM),lead to an excellent stabilization of the at least one oxidizing agent,in particular of hydrogen peroxide. It is therefore advantageous in thecontext of the present disclosure if the cosmetic composition (KM)contains at least one C₁₀-C₃₀ alcohol selected from the group of linearC₁₀-C₂₈ alcohols, linear C₁₂-C₂₆ alcohols, linear C₁₄-C₂₀ alcohols,linear C₁₄-C₁₈ alcohols as well as mixtures of the above-mentionedalcohols, in particular a linear C₁₄-C₁₈ alcohol or a mixture of linearC₁₄-C₁₈ alcohols. In the context of the present disclosure, the mixtureof cetyl alcohol and stearyl alcohol known as cetearyl alcohol, inparticular a mixture of about 50% by weight of cetyl alcohol and about50% by weight of stearyl alcohol, based on the total weight of themixture, has proved to be particularly advantageous. Furthermore, theuse of a linear C₁₄-C₁₈ alcohol, in particular cetyl alcohol, has provento be particularly advantageous.

The at least one C₈-C₃₀ alcohol is preferably used in certain quantityranges. Preferred embodiments of the present disclosure cosmeticcomposition (KM) contains the at least one C₈-C₃₀ alcohol, in particulara linear C₁₄-C₁₈ alcohol or a mixture of linear C₁₄-C₁₈ alcohols, in atotal amount from about 0.10 to about 7.0% by weight, preferably fromabout 0.50 to about 6.5% by weight, more preferably from about 1.0 toabout 6.0% by weight, in particular from about 1.5 to about 5.0% byweight, based on the total weight of the cosmetic composition (KM). Theuse of the above-mentioned total amounts of at least one C₈-C₃₀ alcohol,in particular of a linear C₁₄-C₁₈ alcohol or of the mixture of linearC₁₄-C₁₈ alcohols, in combination with the other ingredients of thecosmetic composition (KM) leads to a particularly good stabilization ofthe oxidizing agent contained in this composition, in particular ofhydrogen peroxide.

As third essential ingredient c), the cosmetic composition (KM) containsat least one specific anionic surfactant. The use of these surfactantsensures sufficient miscibility of the cosmetic composition (KM) with thepreparation (B) containing the oxidative colorant precursors and alsoensures a high storage stability, since failure of components of thecosmetic composition (KM) is avoided. Preferred embodiments of thepresent disclosure cosmetic composition (KM) contains at least oneanionic surfactant chosen from compounds of the formulaR(OCH₂CH₂)_(n)—OSO₃—X₊, wherein R represents saturated or unsaturatedC₁₂-C₂₀ alkyl radicals, n represents integers from about 25 to about 35and X⁺ represents sodium. An anionic surfactant particularly suitable inthe context of the present disclosure is the compound known under theINCI designation Sodium Coceth-30 Sulfate (CAS No.: 68891-38-3).

To ensure a sufficient dispersion of all ingredients of the cosmeticproduct (KM), at least one anionic surfactant is preferably used incertain total amounts. It is therefore preferred in the context of thepresent disclosure if the cosmetic composition (KM) contains the atleast one anionic surfactant, in particular compounds of the formulaR(OCH₂CH₂)_(n)—OSO₃—X₊, in which R represents saturated or unsaturatedC₁₂-C₂₀ alkyl radicals, n represents integers from about 25 to about 35and X+ represents sodium, in a total amount from about 0.10 to about7.0% by weight, preferably from about 0.10 to about 5.0% by weight, morepreferably from about 0.15 to about 4.0% by weight, in particular fromabout 0.20 to about 3.5% by weight relative to the total weight of thecosmetic composition (KM).

As fourth essential ingredient d), the cosmetic composition (KM)contains at least one non-ionic surfactant. The combination of anionicand non-ionic surfactant gives excellent dispersion of the ingredientsof the cosmetic composition (KM) and thus high storage stability. Inaddition, the use of such surfactant combinations results in goodspreadability, in particular miscibility, of the cosmetic composition(KM) with the preparation (B) containing the oxidative colorantprecursors. It is therefore preferred in the context of the presentdisclosure if the cosmetic composition (KM) contains at least onenon-ionic surfactant selected from the group of (i) ethoxylated and/orpropoxylated alcohols and carboxylic acids having 8 to 30 carbon atomsand 2 to 30 ethylene oxide and/or propylene oxide units per mole ofalcohol, (ii) adducts of 30 to 50 moles of ethylene oxide with castoroil and hydrogenated castor oil, (iii) alkyl polyglucosidescorresponding to the formula R¹O-[G]_(p), wherein R¹ is an alkyl and/oralkenyl radical containing 4 to 22 carbon atoms, G is a sugar unitcontaining 5 or 6 carbon atoms and p is a number from 1 to 10, (iv)monoethanolamides of carboxylic acids containing 8 to 30 carbon atomsand (v) mixtures thereof, more particularly ethoxylated alcoholscontaining 14 to 18 carbon atoms and 20 to 30 ethylene oxide units permole of alcohol. In the formula R¹O-[G]_(p), the index number pindicates the degree of oligomerization (DP), i.e. the distribution ofmono- and oligoglucosides, and stands for a number between 1 and 10.Whereas p must always be an integer in a given compound, and inparticular may assume the values p=1 to 6, the value p for a particularalkyl oligoglucoside is an analytically determined arithmetical quantitywhich usually represents a fractional number. As contemplated herein,alkyl and/or alkenyl oligoglucosides with an average degree ofoligomerization p from about 1.1 to about 3.0 are preferably used. Fromthe point of view of application technology, those alkyl and/or alkenyloligoglucosides are preferred whose degree of oligomerization is lessthan about 1.7 and in particular lies between about 1.2 and about 1.7.The alkyl or alkenyl radical R¹ may be derived from primary alcoholscontaining 4 to 20, preferably 8 to 16 carbon atoms. As contemplatedherein, alkyl oligoglucosides based on hardened C_(12/14) coconutalcohol with a DP of 1-3 are particularly preferred, as they arecommercially available for example under the INCI designation“Coco-Glucoside”. The non-ionic surfactants used with particularpreference in the context of the present disclosure are ethoxylatedalcohols with 14 to 18 carbon atoms and 20 to 30 moles of ethylene oxideunits per mole of alcohol, in particular the compound known under theINCI designation Ceteareth-20 (CAS No.:68439-49-6).

According to a particularly preferred embodiment of the presentdisclosure, the anionic surfactant c) of the cosmetic composition (KM)is a sodium sulphate of a linear C₁₂-C₁₄ alkyl ethoxylate with 30ethylene oxide units per surfactant molecule, for example thecommercially available product Disponil® FES 77, and/or is the non-ionicsurfactant d) of the cosmetic composition (KM) a linear C₁₆-C₁₈ethoxylated alcohol with 20 ethylene oxide units per surfactantmolecule, for example the commercially available product Ceteareth-20.In this particularly preferred embodiment of the present disclosure, itis particularly preferred that the sodium sulfate of a linear C₁₂-C₁₄alkyl ethoxylate with 30 ethylene oxide units per surfactant molecule isadded to the cosmetic composition in an amount of from about 1 to about3% by weight, based on the total weight of the cosmetic composition(KM), is contained in the cosmetic composition (KM), and/or the linearC₁₆-C₁₈ ethoxylated alcohol with 20 ethylene oxide units per surfactantmolecule is contained in the cosmetic composition (KM) in an amount offrom about 0.5 to about 2% by weight, based on the total weight of thecosmetic composition (KM). This combination of features has proven to beparticularly advantageous for solving the problem underlying the presentdisclosure.

In order to ensure a sufficient dispersion of all ingredients of thecosmetic product (KM), at least one non-ionic surfactant is preferablyused in certain total quantities. Preferred embodiments of the presentdisclosure cosmetic composition (KM) contains the at least one non-ionicsurfactant, in particular ethoxylated alcohols and having 14 to 18carbon atoms and 20 to 30 ethylene oxide units per mole of alcohol, in atotal amount of from about 0.10 to about 4.0% by weight, preferably fromabout 0.15 to about 3.8% by weight, more preferably from about 0.20 toabout 3.5% by weight, in particular from about 0.30 to about 2.0% byweight relative to the total weight of the cosmetic composition (KM).

As fifth essential ingredient e), the cosmetic composition (KM) containsat least one specific thickening agent. In this context, copolymers of(meth)acrylic acid and acrylic acid ethyl ester have proved to beparticularly advantageous, since these copolymers ensure sufficientthickening over a long period of time, even under highly acidicconditions and in the presence of an oxidizing agent. The thickeningensures a good handling of the cosmetic composition (KM). In order toensure sufficient thickening, at least one thickening agent ispreferably used in certain quantity ranges. It is therefore advantageousin the context of the present disclosure if the cosmetic composition(KM) contains the at least one thickening agent, in particularcopolymers of (meth)acrylic acid and acrylic acid ethyl ester, in atotal amount of from about 0.20 to about 6.0% by weight, preferably offrom about 0.25 to about 5.5% by weight, more preferably of from about0.30 to about 5.0% by weight, in particular of from about 0.40 to about4.5% by weight, relative to the total weight of the cosmetic composition(KM). In the context of the present disclosure, in particular the use ofcopolymers of (meth)acrylic acid and acrylic acid ethyl ester, which arecommercially available under the trade name Aculyn 33 A, has proved tobe useful.

In the course of the work leading to this present disclosure, it hasbeen found that the use of the aforementioned essential ingredients b)to e) ensures that the cosmetic composition (KM) containing at least oneoxidizing agent may be packaged and stored in the special packaging (VP)without this packaging—which has a barrier layer with a permeationbarrier effect for gases and water vapor—expanding or bursting.

In this context, a very specific combination of the essentialingredients a) to e) of the cosmetic composition (KM) has proven to bebeneficial. In a preferred embodiment, the product as contemplatedherein cosmetic composition (KM) comprises hydrogen peroxide, a mixtureof linear C₁₄-C₁₈ alcohols, an anionic surfactant selected fromcompounds of the formula R(OCH₂CH₂)_(n)—OSO₃—X₊, wherein R representssaturated or unsaturated C₁₂-C₂₀ alkyl, n represents an integer from 25to 35 and X+ represents sodium, an ethoxylated alcohol having 14 to 18carbon atoms and 20 to 30 ethylene oxide units per mole of alcohol, anda copolymer of (meth)acrylic acid and acrylic acid ester.

For further optimization of storage stability, the above-mentionedcompounds are preferably used in certain quantity ranges in thepreparation (KM). Particularly preferred forms fact that the cosmeticcomposition (KM) comprises

-   a) from about 1.5 to about 15% by weight of hydrogen peroxide,-   b) from about 1.5 to about 5.0% by weight of a mixture of linear    C₁₄-C₁₈ alcohols,-   c) from about 0.20 to about 3.5% by weight of an anionic surfactant    selected from compounds of the formula R(OCH₂CH₂)_(n)—OSO₃—X₊,    wherein R represents saturated or unsaturated C₁₂-C₂₀ alkyl    radicals, n represents integers from 25 to 35 and X+ represents    sodium,-   d) from about 0.30 to about 2.0% by weight of an ethoxylated alcohol    having 14 to 18 carbon atoms and 20 to 30 ethylene oxide units per    mole of alcohol, and-   e) from about 0.40 to about 4.5% by weight of a copolymer of    (meth)acrylic acid and acrylic acid ethyl ester.

The cosmetic composition (KM) preferably has an acidic pH value in orderto avoid or reduce decomposition of the oxidizing agent used, inparticular the hydrogen peroxide. It is therefore preferred in thecontext of the present disclosure that the cosmetic composition (KM) hasa pH value (measured at 20° C.) of from about pH 1.5 to about pH 5.0,preferably of from about pH 2.0 to about pH 4.7, more preferably of fromabout pH 2.3 to about pH 4.4, in particular of from about pH 2.5 toabout pH 4.

The composition (KM) contained in the packaging (VP) contains theessential ingredients in an aqueous or aqueous-alcoholic carrier, whichmay be a cream, an emulsion, a gel or a surfactant-containing foamingsolution. In order to achieve the desired properties of these dosageforms, the composition (KM) may also contain additional activeingredients, auxiliary substances and additives.

The composition (KM) may also contain one or more acids to stabilize theoxidizing agent used, especially the hydrogen peroxide. It is thereforepreferred in the context of the present disclosure if the cosmeticcomposition (KM) additionally contains at least one acid selected fromthe group of dipicolin acid, lemon acid, vinegar acid, apple acid, milkacid, wine acid, salt acid, phosphorus acid, pyrophosphor acid and theirsalts, benzoe acid and salts thereof, 1-hydroxyethane-1,1-diphosphonicacid, ethylenediaminetetraacetic acid and salts thereof, sulfuric acidand mixtures, in particular a mixture of dipicolin acid, disodiumpyrophosphate, benzoic acid and salts thereof and1-hydroxyethane-1,1-diphosphonic acid.

A particularly high stabilization of the oxidizing agent, in particularof the hydrogen peroxide, is achieved if the above-mentioned acids areused in specific amounts. It is therefore advantageous in this contextif the at least one acid, in particular the mixture of dipicolin acid,disodium pyrophosphate, and 1-hydroxyethane-1,1-diphosphonic acid, iscontained in a total amount of from about 0.1 to about 3.0% by weight,preferably of from about 0.5 to about 2.5% by weight, more preferably offrom about 0.8 to about 2.0% by weight, in particular of from about 0.9to about 1.5% by weight, based on the total weight of the cosmeticcomposition (KM).

The following tables show particularly preferred forms AF 1 to AF 32 ofthe cosmetic composition (KM) contained in the packaging (VP) (allfigures in % by weight, unless otherwise indicated).

AF 1 AF 2 AF 3 AF 4 Oxidizing agent  0.5-20  1.0-18  1.2-16  1.5-15C₈-C₃₀ alcohol 0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant²⁾0.10-7.0 0.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant 0.10-4.00.15-3.8 0.20-3.5 0.30-2.0 Thickening agent³⁾ 0.20-6.0 0.25-5.5 0.30-5.00.40-4.5 Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 5 AF 6 AF 7AF 8 Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant²⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent³⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 9 AF 10 AF 11 AF 12Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant²⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent³⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 13 AF 14 AF 15 AF 16Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant⁶⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent³⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 17 AF 18 AF 19 AF 20Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant⁶⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant⁷⁾ 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent³⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 21 AF 22 AF 23 AF 24Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant⁶⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant⁷⁾ 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent⁸⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100 AF 25 AF 26 AF 27 AF 28Oxidizing agent⁴⁾  0.5-20  1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾0.10-7.0 0.50-6.5  1.0-6.0  1.5-5.0 Anionic surfactant⁶⁾ 0.10-7.00.10-5.0 0.15-4.0 0.20-3.5 Non-ionic surfactant⁷⁾ 0.10-4.0 0.15-3.80.20-3.5 0.30-2.0 Thickening agent⁸⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5Acid  0.1-3.0  0.5-2.5  0.8-2.0  0.9-1.5 Cosmetic carrier¹⁾ ad 100 ad100 ad 100 ad 100 AF 29 AF 30 AF 31 AF 32 Oxidizing agent⁴⁾  0.5-20 1.0-18  1.2-16  1.5-15 C₈-C₃₀ alcohol⁵⁾ 0.10-7.0 0.50-6.5  1.0-6.0 1.5-5.0 Anionic surfactant⁶⁾ 0.10-7.0 0.10-5.0 0.15-4.0 0.20-3.5Non-ionic surfactant⁷⁾ 0.10-4.0 0.15-3.8 0.20-3.5 0.30-2.0 Thickeningagent⁸⁾ 0.20-6.0 0.25-5.5 0.30-5.0 0.40-4.5 Acid⁹⁾  0.1-3.0  0.5-2.5 0.8-2.0  0.9-1.5 Cosmetic carrier¹⁾ ad 100 ad 100 ad 100 ad 100¹⁾aqueous or aqueous alcoholic carrier ²⁾selected from compounds of theformula R(OCH₂CH₂)_(n)—OSO₃—X⁺, wherein R represents saturated orunsaturated C₈-C₃₀ alkyl radicals, n represents integers from about 10to about 50 and X⁺ represents a physiologically tolerable cation³⁾selected from the group of copolymers of (meth)acrylic acid and(meth)acrylic esters, copolymers of (meth)acrylates and(meth)acrylamides, copolymers of hydroxyethyl (meth)acrylates and(meth)acrylamides, copolymers of (meth)acrylates, (meth)acrylamides andethoxylated (meth)acrylic esters, and mixtures thereof ⁴⁾hydrogenperoxide, amount calculated on 100% hydrogen peroxide ⁵⁾selected from amixture of linear C₁₄-C₁₈ alcohols, especially cetearyl alcohol, andlinear C₁₄-C₁₈ alcohols, especially cetyl alcohol ⁶⁾selected fromcompounds of the formula R(OCH₂CH₂)_(n)—OSO₃—X⁺, wherein R representssaturated or unsaturated C₁₂-C₂₀ alkyl radicals, n represents integersfrom 25 to 35 and X+ represents sodium, in particular Sodium Coceth-30Sulphate ⁷⁾selected from ethoxylated alcohols having 14 to 18 carbonatoms and 20 to 30 ethylene oxide units per mole of alcohol, inparticular Ceteareth-20 ⁸⁾selected from copolymers of (meth)acrylic acidand acrylic acid ethyl ester ⁹⁾mixture of dipicolinic acid, disodiumpyrophosphate and 1-hydroxyethane-1,1-diphosphonic acid

The previously described embodiments AF 1 to 32 are each packaged inpackaging (VP) with the following layout of the multi-layer film (F)(from interior (in contact with the cosmetic composition (KM)) toexterior):

-   a) *Interior*-Layer (P1)-Layer (P2)-Barrier layer (BS)-*Exterior*,-   b) *Interior*-Layer (P1)-Barrier layer (BS)-Layer (P2)-*Exterior*,-   c) *Interior*-Layer (P2)-Layer (P1)-Barrier layer (BS)-*Exterior*,-   d) *Interior*-Layer (P2)-Barrier layer (BS)-Layer (P1)-*Exterior*,-   e) *Interior*-Barrier layer (BS)-Layer (P1)-Layer (P2)-*Exterior*,-   f) *Interior*-Barrier layer (BS)-Layer (P2)-Layer (P1)-*Exterior*,-   g) *Interior*-Layer (P1)-Frst adhesive layer (SK1)-Layer (P2)-Second    adhesive layer (SK2)-Barrier layer (BS)-*Exterior*,-   h) *Interior*-Layer (P1)-Adhesive layer (SK1)-Layer (P2)-Barrier    layer (BS)-*Exterior*,-   i) *Interior*-Layer (P1)-Layer (P2)-Second adhesive layer    (SK2)-Barrier layer (BS)-*Exterior*,-   j) *Interior*-Barrier layer (BS)-First adhesive layer (SK1)-Layer    (P1)-Second adhesive layer (SK2)-Layer (P2)-*Exterior*,-   k) *Interior*-Barrier layer (BS)-Adhesive layer (SK)-Layer    (P1)-Layer (P2)-*Exterior*,-   l) *Interior*-Barrier layer (BS)-Layer (S1)-Adhesive layer    (SK)-Layer (P2)-*Exterior*,-   m) *Interior*-Layer (P1)-First adhesive layer (SK1)-Barrier layer    (BS)-Second adhesive layer (SK2)-Layer (P2)-*Exterior*,-   n) *Interior*-Layer (P1)-Adhesive layer (SK)-Barrier layer    (BS)-Layer (P2)-*Exterior*,-   o) *Interior*-Layer (P1)-Barrier Layer (BS)-Adhesive layer    (SK)-Layer (P2)-*Exterior*.

The products obtained in this way have a high storage stability and awater loss during storage that is within an acceptable range. Noswelling or delamination of the packaging (VP) during storage of thesecosmetic products as contemplated herein was observed.

The product as contemplated herein is used for the purpose of oxidativecolor change. For this purpose, the composition (KM) packaged in thepackaging (VP), which is the oxidizing agent composition, is mixed withat least one further composition (B) to produce the ready-to-use colorchanging agent. To prevent incompatibilities or premature reaction, thecompositions (KM) and (B) are packaged separately.

A particularly preferred product as contemplated herein comprises acomposition (B) separately prepared from composition (KM), whereincomposition (B) contains at least one compound selected from oxidativecolorant precursor, direct dyes, alkalizing agents and mixtures thereof.Preferred products of the present disclosure additionally comprises atleast one second cosmetic composition (KM2) which contains at least onecompound selected from oxidative colorant precursor, direct dyes,alkalizing agents and mixtures thereof and which is packaged separatelyfrom the cosmetic composition (KM).

If oxidative coloration is desired, composition (B) contains at leastone oxidative colorant precursor. Oxidative colorant precursors may bedivided into developers and couplers, whereby the developers are usuallyused in the form of their physiologically compatible salts (e.g. in theform of their hydrochlorides, hydrobromides, hydrogen sulfates orsulfates) due to their greater sensitivity to oxygen. Coupler componentsalone do not form a significant coloration in the course of oxidativecoloration, but always require the presence of developer components.Preferably such agents contain at least one oxidative colorant precursorof the developer type and at least one oxidative colorant precursor ofthe coupler type. Particularly suitable oxidative colorant precursors ofthe developer type are selected from at least one compound from thegroup formed by p-phenylenediamine, p-toluenediamine,2-(2-hydroxyethyl)-p-phenylenediamine,2-(1,2-dihydroxyethyl)-p-phenylenediamine,N,N-bis-(2-hydroxyethyl)-p-phenylenediamine,2-methoxymethyl-p-phenylenediamine,N-(4-amino-3-methylphenyl)-N-[3-(1H-imidazol-1-yl)propyl]amine,N,N′-bis-(2-hydroxyethyl)-N,N′-bis-(4-aminophenyl)-1,3-diamino-propan-2-ol,bis-(2-hydroxy-5-aminophenyl)methane,1,3-bis-(2,5-diaminophenoxy)propane-2-ol,N,N′-bis-(4-aminophenyl)-1,4-diazacycloheptane,1,10-bis-(2,5-diaminophenyl)-1,4,7,10-tetraoxadecane p-Aminophenol,4-amino-3-methylphenol, 4-amino-2-aminomethylphenol,4-amino-2-(1,2-dihydroxyethyl)phenol,4-amino-2-(diethylaminomethyl)phenol4,5-diamino-1-(2-hydroxyethyl)pyrazole, 2,4,5,6-tetraamino-pyrimidine,4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triamino-pyrimidine,2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-on and theirphysiologically compatible salts.

Particularly suitable oxidative colorant precursors of the coupler typeare selected from the group formed by 3-aminophenol,5-amino-2-methylphenol, 3-amino-2-chloro-6-methylphenol,2-hydroxy-4-aminophenoxyethanol, 5-amino-4-chloro-2-methylphenol,5-(2-hydroxyethyl)-amino-2-methylphenol, 2,4-dichloro-3-aminophenol,2-aminophenol, 3-phenylene-diamine, 2-(2,4-diaminophenoxy)ethanol,1,3-bis(2,4-diaminophenoxy)propane,1-methoxy-2-amino-4-(2-hydroxyethylamino)benzene,1,3-bis(2,4-diaminophenyl)propane,2,6-bis(2′-hydroxyethylamino)-1-methylbenzene,2-({3-[(2-hydroxyethyl)amino]-4-methoxy-5-methylphenyl}amino)ethanol,2-({3-[(2-hydroxyethyl)amino]-2-methoxy-5-methylphenyl}amino)ethanol,2-({3-[(2-hydroxyethyl)amino]-4,5-dimethylphenyl}amino)ethanol,2-[3-morpholin-4-ylphenyl)amino]ethanol,3-amino-4-(2-methoxy-ethoxy)-5-methylphenylamine,1-amino-3-bis-(2-hydroxyethyl)aminobenzene, resorcinol,2-methylresorcinol, 4-chlororesorcinol, 1,2,4-trihydroxybenzene,2-amino-3-hydroxypyridine, 3-amino-2-methylamino-6-methoxypyridine,2,6-dihydroxy-3,4-dimethylpyridine, 3,5-diamino-2,6-dimethoxypyridine,1-phenyl-3-methylpyrazol-5-on, 1-naphthol, 1,5-dihydroxy-naphthalene,2,7-dihydroxynaphthalene, 1,7-dihydroxynaphthalene,1,8-dihydroxy-naphthalene, 4-hydroxy-indole, 6-hydroxyindole,7-hydroxyindole, 4-hydroxyindoline, 6-hydroxyindoline, 7-hydroxyindolineor mixtures of these compounds or their physiologically acceptablesalts.

In addition, the composition (B) may also contain one or more directdyes. Suitable non-ionic direct dyes may be selected from the group HCYellow 2, HC Yellow 4, HC Yellow 5, HC Yellow 6, HC Yellow 12, HC Orange1, Disperse Orange 3, HC Red 1, HC Red 3, HC Red 7, HC Red 10, HC Red11, HC Red 13, HC Red BN, HC Blue 2, HC Blue 11, HC Blue 12, DisperseBlue 3, HC Violet 1, Disperse Violet 1, Disperse Violet 4, DisperseBlack 9, 1,4-diamino-2-nitrobenzene, 2-amino-4-nitrophenol,1,4-bis(2-hydroxyethyl)-amino-2-nitrobenzene,3-nitro-4-(2-hydroxyethyl)aminophenol,2-(2-hydroxyethyl)amino-4,6-dinitro-phenol,4-[(2-hydroxyethyl)amino]-3-nitro-1-methylbenzene,1-amino-4-(2-hydroxyethyl)amino-5-chloro-2-nitrobenzene,4-amino-3-nitrophenol, 1-(2′-ureidoethyl)amino-4-nitrobenzene,2-[(4-amino-2-nitrophenyl)amino]benzoic acid,4-[(3-hydroxypropyl)amino]-3-nitrophenol, 4-nitro-o-phenylenediamine,6-nitro-1,2,3,4-tetrahydroquinone, 2-hydroxy-1,4-naphthoquinone,picramine acid and its salts, 2-amino-6-chloro-4-nitrophenol,4-ethylamino-3-nitrobenzoe acid and 2-chloro-6-ethylamino-4-nitrophenol.

Suitable anionic direct dyes may be selected from the group includingAcid Yellow 1, Yellow 10, Acid Yellow 23, Acid Yellow 36, Acid Orange 7,Acid Red 33, Acid Red 52, Pigment Red 57:1, Acid Blue 7, Acid Green 50,Acid Violet 43, Acid Black 1, Acid Black 52, Bromophenol Blue andTetrabromophenol Blue.

Suitable cationic direct dyes are cationic triphenylmethane dyes, suchas Basic Blue 7, Basic Blue 26, Basic Violet 2 and Basic Violet 14,aromatic systems substituted with a quaternary nitrogen group, such asBasic Yellow 57, Basic Red 76, Basic Blue 99, Basic Brown 16 and BasicBrown 17, cationic anthraquinone dyes, such as HC Blue 16 (Bluequat B),and direct dyes containing a heterocycle containing at least onequaternary nitrogen atom, in particular Basic Yellow 87, Basic Orange 31and Basic Red 51. The cationic direct dyes marketed under the trademarkArianor are also suitable cationic direct dyes as contemplated herein.

Dyeing processes on keratinous fibers are usually carried out in analkaline environment. In order to protect the keratinous fibers and alsothe skin as much as possible, however, the adjustment of a too high pHvalue is not desirable. Therefore, it is preferable if the pH value ofcomposition (B) is between about 7 and about 11, especially betweenabout 8 and about 10.5. For the purposes of the present disclosure, thepH values are pH values measured at a temperature of 22° C.

Composition (B) may contain at least one alkalizing agent. Thealkalizing agents usable for adjusting the preferred pH value ascontemplated herein may be selected from the group formed by ammonia,alkanolamines, basic amino acids, and inorganic alkalizing agents suchas (earth) alkali metal hydroxides, (earth) alkali metal metasilicates,(earth) alkali metal phosphates and (earth) alkali metal hydrogenphosphates. Preferred inorganic alkalizing agents are magnesiumcarbonate, sodium hydroxide, potassium hydroxide, sodium silicate andsodium metasilicate. Organic alkalizing agents which can be used ascontemplated herein are preferably selected from monoethanolamine,2-amino-2-methyl-propanol and triethanolamine. The basic aminoacidsusable as alkalizing agents as contemplated herein are preferablyselected from the group formed from arginine, lysine, ornithine andhistidine, especially preferably arginine. However, in the course of theinvestigations into the present disclosure, it was found that furtheragents preferred as contemplated herein are exemplified by the fact thatthey additionally contain an organic alkalizing agent. An embodiment ofthe first present disclosure agent additionally contains at least onealkalizing agent selected from the group formed by ammonia,alkanolamines and basic aminoacids, in particular ammonia,monoethanolamine and arginine or its compatible salts.

The composition (B) may further contain additional active ingredients,auxiliary substances and additives. For example, one or more fatcomponents from the group of C₁₂-C₃₀ fatty alcohols, C₁₂-C₃₀ fatty acidtriglycerides, C₁₂-C₃₀ fatty acid monoglycerides, C₁₂-C₃₀ fatty aciddiglycerides and/or hydrocarbons may be included.

Preferably, a surface-active substance may be added to composition (B),whereby such surface-active substances are referred to as surfactants oremulsifiers, depending on the area of application: they are preferablyselected from anionic, zwitterionic, amphoteric and non-ionicsurfactants and emulsifiers.

The composition (B) preferably contains at least one anionic surfactant.Preferred anionic surfactants are fatty acides, alkyl sulfates, alkylether sulfates and ether carbon acids with 10 to 20 carbon atoms in thealkyl group and up to 16 glycol ether groups in the molecule.

Furthermore, composition (B) may additionally contain at least onezwitterionic surfactant. Preferred zwitterionic surfactants arebetaines, N-alkyl-N,N-dimethylammonium-glycinate,N-acyl-aminopropyl-N,N-dimethylammoniumglycinate, and2-alkyl-3-carboxymethyl-3-hydroxyethyl-imidazolines. A preferredzwitterionic surfactant is known under the INCI designationCocamidopropyl Betaine.

Furthermore, it may be intended that the composition (B) contains atleast one amphoteric surfactant. Preferred amphoteric surfactants areN-alkyl glycines, N-alkylpropionic acids, N-alkyl-aminobutter acids,N-alkyl aminodipropionacids, N-hydroxyethyl-N-alkylamidopropylglycines,N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids andalkylaminoaceticacids. Particularly preferred amphoteric surfactants areN-coconut alkylaminopropionate, as coconut acylaminoethylaminopropionate and C₁₂-C₁₈ acyl sarcosine.

Furthermore, it has proven to be advantageous if the composition (B)contains further, non-ionic surface-active substances. Preferrednon-ionic surfactants are alkyl polyglycoside and alkylene oxide plantproducts on fatty alcohols and fatty acids with 2 to 30 moles ofethylene oxide per mole of fatty alcohol or fatty acid. Compositionswith outstanding properties are also obtained if they contain fatty acidesters of ethoxylated glycerol as non-ionic surfactants.

The non-ionic, zwitterionic or amphoteric surfactants are used inproportions of from about 0.1 to about 45% by weight, preferably fromabout 1 to about 30% by weight and particularly preferably from about 1to about 15% by weight, based on the total weight of the composition(B).

Composition (B) may also contain at least one thickening agent. Thereare no restrictions in principle with regard to these thickening agents.Both organic and purely inorganic thickening agents may be used.Suitable thickening agents are anionic, synthetic polymers, cationic,synthetic polymers, naturally occurring thickening agents such asnon-ionic guar gums, scleroglucan gums or xanthane gums, gum arabicum,ghatti gum, karaya gum, tragacanth gum, carrageenan gum, agar-agar,carob bean gum, pectins, alginates, starch fractions and derivativessuch as amylose, amylo-pectin and dextrine, as well as cellulosederivatives such as methyl cellulose, carboxyalkyl celluloses andhydroxyalkyl celluloses, non-ionic, fully synthetic polymers such aspolyvinyl alcohol or polyvinyl pyrrolidinone as well as inorganicthickening agents, in particular phyllosilicates such as bentonite,especially smectites such as montmorillonite or hectorite.

Furthermore, composition (B) may contain other active ingredients,auxiliary substances and additives, such as non-ionic polymers such asvinylpyrrolidine/vinyl acrylat copolymers, polyvinylpyrrolidinone,vinylpyrrolidine/vinyl acetate copolymers, polyethylene glycols andpoly-siloxanes; additional silicones such as volatile or non-volatile,straight-chain, branched or cyclic, crosslinked or non-crosslinkedpolyalkylsiloxanes (such as dimethicones or cyclomethicones),polyarylsiloxanes and/or polyalkylarylsiloxanes, in particularpolysiloxanes with organo-functional groups, such as substituted orunsubstituted amines (amodimethicones), carboxyl, alkoxy and/or hydroxylgroups (dimethicone copolyols), linearpolysiloxane(A)-polyoxyalkylene(B) block copolymers, grafted siliconepolymers; cationic polymers such as quaternized cellulose ethers,polysiloxanes with quaternary groups, dimethyldiallylammonium chloridepolymers, acrylamidedimethyldiallylammonium chloride copolymers,dimethylamino-ethyl methacrylate-vinylate vinyl pyrrolidinone copolymersquaternized with diethyl sulfate, vinyl pyrrolidinone-imidazoliummethochloride copolymers and quaternized polyvinyl alcohol; zwitterionicand amphoteric polymers; anionic polymers such as, for example,polyacrylacids or cross-linked polyacrylics; structurants such asglucose, maleic acid and lactic acid, hair-conditioning compounds suchas phospholipids, for example lecithin and cephalins; perfume oils,dimethyl iso-sorbide and cyclodextrins; fiber structure-improving activesubstances, in particular mono-, di- and oligo-saccharides such asglucose, galactose, fructose, fructose and lactose; dyes for colouringthe composition; anti-dandruff active substances such as piroctoneolamines, zinc omadine and climbazole; amino acids and oligopeptides;animal and/or vegetable-based protein hydrolysates, as well as in theform of their fatty acid condensation products or optionally anionicallyor cationically modified derivatives; fatty substances and vegetableoils; sunscreens and UV blockers; active ingredients such as panthenol,panthenic acid, pantolactone, allantoin, pyrrolidinone-carbon acid andits salts, and bisabolol; polyphenols, in particular hydroxyzimtacids,6,7-dihydroxycoumarins, hydroxybenzoeacids, catechins, tannins,leucoanthocyanidins, anthocyanidins, flavanones, flavones and flavonols;ceramides or pseudoceramides; vitamins, provitamins and vitaminprecursors; plant extracts; fats and waxes such as fatty alcohols,beeswax, montan wax and paraffins; swelling and penetrating agents suchas glycerine, propylene glycol monoethyl ether, carbonates, hydrogencarbonates, guanidines, ureas as well as primary, secondary and tertiaryphosphates; anti-caking agents such as latex, styrene/PVP andstyrene/acrylamide copolymers; pearlescent agents such as ethyleneglycol mono- and distearate as well as PEG-3 distearate and pigments.

The selection of these additional substances will be made by the expertaccording to the desired properties of the composition (B) as well asthe product as contemplated herein. With regard to further optionalcomponents and the quantities of these components used, explicitreference is made to the relevant handbooks known to the expert. Theadditional active ingredients and auxiliary substances are preferablyused in the composition (B) in quantities of from about 0.0001 to about25% by weight each, in particular from about 0.0005 to about 15% byweight, in each case based on the total weight of the composition (B).

The following examples explain the present disclosure without limitingit:

Examples

A 100 nm thick layer of aluminum was vapor-deposited onto a film layerof biaxially oriented polypropylene with a thickness of 12 μm(micrometer). The aluminum layer was then painted over with approx. 3g/m² of ORMOCER polymer and cured. A 70 μm (micrometer) thick layer ofpolyethylene was then applied to the ORMOCER layer. A packaging (VP) wasproduced from the film. The film is also provided with a PET layer 20 μmthick.

The following cosmetic compositions (KM) were used (all figures in % byweight):

Ingredients KM Sodium hydroxide (50%) 0.72 Dipicolinic acid 0.10Disodium pyrophosphate 0.030 1-hydroxyethane-1,1-diphosphonic acid (60%)1.5 Oxidizing agent¹⁾ 10 Cs-Cao alcohol²⁾ 3.5 Anionic surfactant³⁾ 2.5Non-ionic surfactant⁴⁾ 1.0 Thickening agent⁵⁾ 10 Water ad 100¹⁾preferably hydrogen peroxide, calculated on 100% H₂O₂ ²⁾preferably alinear C₁₄—C₁₈ alcohol, especially cetyl alcohol ³⁾preferably a sodiumsalt of C₁₆—C₁₈ alkysulfates substituted with oxyethylene groupsespecially Disponil ® FES 77 ⁴⁾preferably a C₁₆—C₁₈ alkyl ethersubstituted with oxyethylene, especially Ceteareth-20, ⁵⁾preferably acopolymer of (meth)acrylic acid and acrylic acid ethyl ester, especiallyAculyr 33 A

Ingredients KM Ammonia (25%) 0.65 Dipicolinic acid 0.10 Disodiumpyrophosphate 0.030 1-hydroxyethane-1,1-diphosphonic acid (60%ig) 1.5Oxidizing agent¹⁾ 12 C₈—C₃₀ alcohol²⁾ 3.5 Anionic surfactant³⁾ 2.5Non-ionic surfactant⁴⁾ 1.0 Thickening agent⁵⁾ 10 Water ad 100¹⁾preferably hydrogen peroxide, calculated on 100% H₂O₂ ²⁾preferably alinear C₁₄—C₁₈ alcohol, especially cetyl alcohol ³⁾preferably a sodiumsalt of C₁₆—C₁₈ alkysulfates substituted with oxyethylene groups,especially Disponil ® FES 77 ⁴⁾preferably a C₁₆—C₁₈ alkyl ethersubstituted with oxyethylene, especially Ceteareth-20, ⁵⁾preferably acopolymer of (meth)acrylic acid and acrylic acid ethyl ester, especiallyAculyn 33 A

The cosmetic composition KM was filled in the previously describedpackaging (VP). Then the packaging was stored at 40° C. for 24 weeks.The packaging was not inflated or delaminated.

While at least one exemplary embodiment has been presented in theforegoing detailed description, it should be appreciated that a vastnumber of variations exist. It should also be appreciated that theexemplary embodiment or exemplary embodiments are only examples, and arenot intended to limit the scope, applicability, or configuration of thevarious embodiments in any way. Rather, the foregoing detaileddescription will provide those skilled in the art with a convenient roadmap for implementing an exemplary embodiment as contemplated herein. Itbeing understood that various changes may be made in the function andarrangement of elements described in an exemplary embodiment withoutdeparting from the scope of the various embodiments as set forth in theappended claims.

1. A cosmetic product for modifying the natural color of keratinousfibers comprising (i) at least one packaging comprising at least onemulti-layer film comprising at least one first polymer layer, at leastone second polymer layer and at least one barrier layer, and (ii) atleast one cosmetic composition packaged in the packaging and comprising:a) at least one oxidizing compound, b) at least one C₈-C₃₀ alcohol, c)at least one anionic surfactant selected from compounds of the formulaR(OCH₂CH₂)_(n)—OSO₃—X⁺, wherein R represents saturated or unsaturatedC₈-C₃₀ alkyl radicals, n represents integers from 10 to 50 and X⁺represents a physiologically tolerable cation, d) at least one non-ionicsurfactant, and e) at least one thickening agent selected from the groupof copolymers of (meth)acrylic acid and (meth)acrylic esters, copolymersof (meth)acrylates and (meth)acrylamides, copolymers of hydroxyethyl(meth)acrylates and (meth)acrylamides, copolymers of (meth)acrylates,(meth)acrylamides and ethoxylated (meth)acrylic acid esters and mixturesthereof wherein the first polymer layer is formed of polyethyleneterephthalate or polyethylene naphthalate, the second polymer layer isformed of a polyolefin and the barrier layer is formed of metalized,oriented polypropylene.
 2. The cosmetic product according to claim 1,wherein the first polymer layer has a layer thickness of from about 4 μmto about 50 μm; the second polymer layer has a layer thickness of fromabout 20 μm to about 150 μm; and/or the barrier layer has a layerthickness of from about 4 μm to about 20 μm.
 3. The cosmetic productaccording to claim 1, wherein the multi-layer film has an OxygenTransmission Rate at 23° C. and 50% relative humidity of from about 0.1to 5 cc/m²/d/bar and has a water vapor permeability at 38° C. and 100%relative humidity of from about 0.1 to about 5 g/m²d.
 4. The cosmeticproduct according to claim 1, wherein the adhesive strength of the filmis from about 0.1 to about 10 N/15 mm and/or wherein the seal strengthof the packaging is from about 10 to about 40 N/15 mm under theconditions 150° C., 2.54 cm (1″) and 4 kg/cm².
 5. The cosmetic productaccording to claim 1, wherein the at least one barrier layer is disposedbetween the at least one first polymer layer and the at least one secondpolymer layer.
 6. The cosmetic product according to claim 1, wherein thefirst polymer layer forms an outer layer of the at least one packaging.7. The cosmetic product according to claim 1, wherein the cosmeticcomposition has a pH value (measured at 20° C.) of from about 1.5 toabout 5.0.
 8. The cosmetic product according to claim 1, wherein thecosmetic composition comprises the at least one oxidizing compound in atotal amount from about 0.5 to about 20% by weight and/or wherein thecosmetic composition comprises the at least one C₈-C₃₀ alcohol in atotal amount from about 0.10 to about 7.0% by weight.
 9. The cosmeticproduct according to claim 1, wherein the cosmetic composition comprisesthe at least one thickening agent e) in a total amount from about 0.2 toabout 6% by weight.
 10. The cosmetic product according to claim 1,wherein the anionic surfactant c) of the cosmetic composition is asodium sulphate of a linear C₁₂-C₁₄ alkyl ethoxylate with 30 ethyleneoxide units per surfactant molecule, and/or the non-ionic surfactant d)of the cosmetic composition is a linear C₁₆-C₁₈ ethoxylated alcohol with20 ethylene oxide units per surfactant molecule.
 11. The cosmeticproduct according to claim 1, wherein the anionic surfactant c) of thecosmetic composition is a sodium sulphate of a linear C₁₂-C₁₄ alkylethoxylate with 30 ethylene oxide units per surfactant molecule.
 12. Thecosmetic product according to claim 11, wherein the sodium sulfate of alinear C₁₂-C₁₄ alkyl ethoxylate having 30 ethylene oxide units persurfactant molecule is included in the cosmetic composition in an amountof 1 to 3% by weight, based on the total weight of the cosmeticcomposition.
 13. The cosmetic product according to claim 1, wherein thenon-ionic surfactant d) of the cosmetic composition is a linear C₁₆-C₁₈ethoxylated alcohol with 20 ethylene oxide units per surfactantmolecule.
 14. The cosmetic product according to claim 13, wherein thelinear C₁₆-C₁₈ ethoxylated alcohol with 20 ethylene oxide units persurfactant molecule is included in the cosmetic composition in an amountof from about 0.5 to about 2% by weight, based on the total weight ofthe cosmetic composition.
 15. The cosmetic product according to claim 1,wherein the first polymer layer (P1) has a layer thickness of from about5 μm to about 35 μm.
 16. The cosmetic product according to claim 1,wherein the first polymer layer (P1) has a layer thickness of from about6 μm to about 20 μm.
 17. The cosmetic product according to claim 1,wherein the second polymer layer (P2) has a layer thickness of fromabout 30 μm to about 110 μm.
 18. The cosmetic product according to claim1, wherein the second polymer layer (P2) has a layer thickness of fromabout 40 μm to about 90 μm.
 19. The cosmetic product according to claim1, wherein the barrier layer (BS) has a layer thickness of from about 5μm to about 18 μm.
 20. The cosmetic product according to claim 1,wherein the barrier layer (BS) has a layer thickness of from about 6 μmto about 15 μm.